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Nookie1986 [14]
3 years ago
7

Explain why a viral infection can't be treated with antibiotics ​

Biology
1 answer:
elena-s [515]3 years ago
7 0

Antibiotics take their effect on bacteria, precisely on their metabolism. To understand why they work on bacteria but not on viruses you must first understand the basics of how each parasite behaves, is structured and, affects the infected individual. Bacteria use ribosomes to synthesize proteins some antibiotics inhibit protein synthesis, therefore the bacteria is killed. Bacteria can evolve into becoming resistant to antibiotics by synthesizing an inactivator enzyme that cancels the effect of the antibiotic. Most bacteria affect people by releasing toxins. Viruses don't have a metabolism, one of the main reasons why they're not considered living things. They use the guest to replicate by inserting their genetic material DNA(adenoviruses) or RNA(riboviruses) inside the cell. They use the cell to multiply. Viruses are made of the mentioned genetic material(RNA or DNA) and a capsid(a capsule that encloses the genetic material). It affects the sick person by multiplying inside cells so many times, eventually making them burst, releasing thousands of viruses and, by causing an immune reaction.

To summarize antibiotics work on bacteria and not on viruses because bacteria have a metabolism that can be inhibited and viruses don't.

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When health care teams solve problems, it is important that in the final stage, all team members _____. Have a say in the goals
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The correct answer is ''understand their roles''

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Critical protein-protein interactions within the CARMA1-BCL10-MALT1 complex: Take-home points for the cell biologist
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Protein-protein interactions within the CARMA1-BCL10-MALT1 complex:

  • The T-cell receptor and B-cell receptor-dependent NF-B induction and lymphocyte activation are mediated by the CBM complex, which is made up of the proteins CARMA1, BCL10, and MALT1.
  • Each of the proto-oncoproteins CARMA1, BCL10, and MALT1 is a somatic gain-of-function mutation or chromosomal translocation, and dysregulation of CBM signaling is a characteristic of numerous lymphoid malignancies, including Activated B-cell Diffuse Large B-cell Lymphoma.
  • Moreover, a number of immunological dysregulation diseases have been linked to both gain- and loss-of-function germline mutations in CBM complex proteins.
  • Over the past ten years, careful examination of the interactions of CBM components has yielded a wealth of detailed structural knowledge.
  • Here, we discuss important discoveries about the molecular nature of these protein-protein interactions that have helped the research develop a detailed understanding of how these proteins come together to form high-order filamentous CBM complexes.
  • Approaches to therapeutic suppression of the CBM complex have thus far centered on obstructing MALT1 protease activity in order to treat lymphoid malignancy and/or autoimmunity.
  • The structural effects of MALT1 protease inhibitors on significant protein-protein interactions are also reviewed in detail.

To learn more about protein-protein interaction visit:

brainly.com/question/14573382

#SPJ4

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